Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1036332
rs1036332
3 1 199043349 intron variant A/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs111759324
rs111759324
2 1 101186966 upstream gene variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs11204682
rs11204682
4 1 150623061 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs114269697
rs114269697
3 1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11579220
rs11579220
1 1 205175235 intron variant G/T snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs12075
rs12075
22 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 0.700 1.000 1 2016 2016
dbSNP: rs12239046
rs12239046
9 1 247438293 intron variant T/C snv 0.58 0.700 1.000 1 2016 2016
dbSNP: rs12408934
rs12408934
2 1 64957764 intron variant G/A snv 6.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs12748961
rs12748961
2 1 205707135 intergenic variant T/C snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs12752838
rs12752838
4 1 8853597 upstream gene variant A/G snv 0.54 0.700 1.000 1 2016 2016
dbSNP: rs146091102
rs146091102
2 1 26795439 intron variant G/A snv 2.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs1537061
rs1537061
1 1 87273536 regulatory region variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs1754541
rs1754541
2 1 101160327 intergenic variant A/G snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs17592479
rs17592479
4 1 226986191 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs1999537
rs1999537
2 1 56439852 intron variant G/A snv 0.89 0.700 1.000 1 2016 2016
dbSNP: rs201950044
rs201950044
5 1 161639782 intergenic variant G/T snv 0.700 1.000 1 2016 2016
dbSNP: rs2072735
rs2072735
2 1 9295413 intron variant A/C snv 0.76 0.700 1.000 1 2016 2016
dbSNP: rs2147904
rs2147904
2 1 41905743 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs2208568
rs2208568
5 1 235926855 intergenic variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2296618
rs2296618
2 1 198697103 intron variant A/G snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs2476601
rs2476601
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.700 1.000 1 2016 2016
dbSNP: rs2814778
rs2814778
24 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs301807
rs301807
4 0.925 0.080 1 8424763 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3123543
rs3123543
13 1 212617344 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs3218192
rs3218192
2 1 23514878 intron variant G/T snv 0.40 0.700 1.000 1 2016 2016